Recalls affecting Vermont
Notices that name Vermont in their distribution area, plus every nationwide recall — nationwide recalls reach Vermont too.
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Class II · 11 months ago
Bard Peripheral Vascular Inc Safe-T-Centesis 6 Fr Catheter Drainage Tray recall: Acute drainage catheters, indicated for use in removing fluid during acute
Acute drainage catheters, indicated for use in removing fluid during acute drainage/aspiration procedure, manufactured with safety indicators that…
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Class III · 11 months ago
Orthofix U.S. LLC Brand Name: Construx" Mini PTC Spacer System Product Name: Construx" recall: Labeling contains claims that are not consistently present
Labeling contains claims that are not consistently present.
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Class III · 11 months ago
Orthofix U.S. LLC Brand Name: Construx" Mini Ti Spacer System Product Name: Construx" recall: Labeling contains claims that are not consistently present
Labeling contains claims that are not consistently present.
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Class II · 11 months ago
C.R. Bard Inc BD InLay Optima Ureteral Stent Kit Size: 4.7 Fr. x 26 cm recall: Labeling discrepancy; Ureteral stent actual size may not match the actual
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
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Class II · 11 months ago
Datascope Corp. Cardiosave Hybrid. Intra-Aortic Balloon Pump system recall: The IFU addendum revises the Preventative Maintenance schedule to align
The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.
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Class II · 11 months ago
Cardinal Health 200, LLC ChemoPlus gowns: Product Code recall: Affected gowns have the incorrect expiration date on the product packaging
Affected gowns have the incorrect expiration date on the product packaging. Product has a shelf-life of three years which is mislabeled on the…
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Class II · 11 months ago
Beckman Coulter, Inc. Access 2 Reaction Vessels, individual, disposable recall: It has been determined that certain lots of Access 2 Reaction Vessels
It has been determined that certain lots of Access 2 Reaction Vessels may contain manufacturing deformities. The bottom (round end) of the Reaction…
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Class II · 11 months ago
C.R. Bard Inc Bard InLay Optima Size: 6 Fr. x 14 cm, Ureteral Stent Kit REF 787614 recall: Labeling discrepancy; Ureteral stent actual size may not match the actual
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
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Class III · 11 months ago
Orthofix U.S. LLC Brand Name: Forza" Ti Spacer System Product Name: Forza" Ti Spacer recall: Labeling contains claims that are not consistently present
Labeling contains claims that are not consistently present.
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Class II · 11 months ago
C.R. Bard Inc BD InLay Optima Ureteral Stent Kit Size: 6 Fr. x 30 cm recall: Labeling discrepancy; Ureteral stent actual size may not match the actual
Labeling discrepancy; Ureteral stent actual size may not match the actual product label.
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Class II · 11 months ago
Steris Corporation AMSCO 7053HP Washer/Disinfector Model/ recall: Wire connected to the electrical box may shift out of its intended position
Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains…
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Class II · 11 months ago
Steris Corporation AMSCO 7052HP Washer/Disinfector Model/ recall: Wire connected to the electrical box may shift out of its intended position
Wire connected to the electrical box may shift out of its intended position, which may result in electrical arcing. Electrical arcing remains…
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Class II · 11 months ago
Datascope Corp. Cardiosave Rescue. Intra-Aortic Balloon Pump system recall: The IFU addendum revises the Preventative Maintenance schedule to align
The IFU addendum revises the Preventative Maintenance schedule to align with the update introduced in the Service Manual as of June 2023.
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Class II · 11 months ago
Fagron Compounding Services Tropicamide 1%/Cyclopentolate 1%/Phenylephrine recall: Incorrect Product Formulation
Incorrect Product Formulation
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Class III · 11 months ago
Glenmark Pharmaceuticals Inc., USA Nebivolol Tablets, 20 mg, 90 Tablets recall: Cross Contamination with Other Products
Cross Contamination with Other Products
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Class II · 11 months ago
Cipla USA, Inc. Cinacalcet Hydrochloride Tablets, 60 mg, 30 Tablets per bottle recall: CGMP Deviations: the presence of a nitrosamine impurity
CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
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Class II · 11 months ago
Cipla USA, Inc. Lanthanum Carbonate chewable tablets, 1000mg* recall: Failed stability specifications: Out of specification for hardness test
Failed stability specifications: Out of specification for hardness test
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Class II · 11 months ago
Cipla USA, Inc. Cinacalcet Hydrochloride Tablets, 30 mg, 30 Tablets per bottle recall: CGMP Deviations: the presence of a nitrosamine impurity
CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
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Class II · 11 months ago
Cipla USA, Inc. Cinacalcet Hydrochloride Tablets, 90 mg, 30 Tablets per bottle recall: CGMP Deviations: the presence of a nitrosamine impurity
CGMP Deviations: the presence of a nitrosamine impurity, N-nitroso-cinacalcet, above the acceptable daily intake (ADI) limits.
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Class II · 11 months ago
Lupin Pharmaceuticals Inc. Sertraline Hydrochloride Tablets USP, 100 mg recall: Defective container - seal not adhering to bottles
Defective container - seal not adhering to bottles
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Class III · 11 months ago
Winder Laboratories, LLC Morphine Sulfate Oral Solution 100 mg / 5 mL , 30 mL recall: Correct Labeled Product Mispack-Size stated on carton label did not match
Correct Labeled Product Mispack-Size stated on carton label did not match the size of the bottle in the carton.
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Class III · 11 months ago
Dr. Reddy's Laboratories, Inc. Varenicline Tablets, 1mg, 56 Tablets recall: Sub potent drug: during the 9-month stability test conducted
Sub potent drug: during the 9-month stability test conducted, the assay value for the affected lot was below specification limit.
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Class II · 11 months ago
Cipla USA, Inc. Lanthanum Carbonate chewable tablets, 1000mg* recall: Failed stability specifications: Out of specification for hardness test
Failed stability specifications: Out of specification for hardness test
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NHTSA safety recall · 11 months ago
Toyota Camry Hybrid and Corolla Cross Hybrid recall: A bolt inside the inverter may not have been tightened properly
A bolt inside the inverter may not have been tightened properly, causing incomplete contact at the inverter terminal.